A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067426



Internal ID21976659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69474072..69474072hg38UCSC Ensembl
chr8:70386307..70386307hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587816
Samples
Known GenesSULF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067426
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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